Association of polymorphisms of HSD11B1 and ACE genes with trachoma disease [0.03%]
HSD11B1和ACE基因多态性与沙眼的关系研究
Laura L Valdez-Velazquez,Héctor Ochoa-Díaz-López,Iván Delgado-Enciso et al.
Laura L Valdez-Velazquez et al.
Trachoma, caused by Chlamydia trachomatis, is the most common infectious blindness in the world and is present in indigenous Mayan from Chiapas (Mexico). Inflammatory genes are activated when suffering from trachoma, thus some polymorphisms...
Extraction of genomic DNA for sequencing from snail Helix lucorum [0.03%]
来自蜗牛Helix lucorum的测序基因组DNA的提取
Dmitry Panteleev,Anastasia Sadova,Galina Pavlova
Dmitry Panteleev
Genomic studies make it possible to breakthrough in many fields such as biochemistry, physiology, phylogenetics, etc., though they are unworkable without sequences of genomic DNA of an organism. The terrestrial mollusks’ genomes would bene...
Case Reports
Journal of genetics. 2024:103:20. DOI: 2024
Wei-Liang Liu,Fang Li,Lu Liu et al.
Wei-Liang Liu et al.
In the past, there were no easily distinct and recognizable features as a guide for precise clinical and genetic diagnosis of cases with chromosome microdeletions involving 15q26 including CHD2,. The present study analysed the clinical data...
Case Reports
Journal of genetics. 2024:103:21. DOI: 2024
Mitogenome features and phylogenetic analysis of red algae, Grateloupia cornea (Rhodophyta, Halymeniales) [0.03%]
Grateloupia cornea（Rhodophyta，Halymeniales）的线粒体基因组特征及系统发育分析
Maheshkumar Prakash Patil,Young-Ryun Kim,Shinya Nakashita et al.
Maheshkumar Prakash Patil et al.
The mitogenome is an important tool for taxonomic and evolutionary investigation. Here, a few complete mitogenomes of red algae have been reported. We have reported the complete mitogenome sequences of Grateloupia cornea Okamura, 1913 (Rhod...
The first complete mitochondrial genome of the critically endangered Malaysian giant turtle, Orlitia borneensis (Testudines: Geoemydidae) [0.03%]
马来西亚濒危巨龟奥氏弹涂龟的第一个完整线粒体基因组序列(Testudines: Geoemydidae)
Mohd Hairul Mohd Salleh,Yuzine Esa
Mohd Hairul Mohd Salleh
We present here the complete mitochondrial sequence of the critically endangered Malaysian giant turtle, Orlitia borneensis. The assembled mitochondrial genome includes 13 protein-coding genes (PCGs), 22 transfer RNA (tRNA) genes, two ribos...
Foetal haemoglobin elevation, unfavourable prognosis, and protective role of genetic variants HBG2 rs7482144, HBS1L-MYB rs9399137 and BCL11A rs4671393 in children with ALL [0.03%]
胎儿血红蛋白升高、不良预后及其基因多态性HBG2 rs7482144、HBS1L-MYB rs9399137和BCL11A rs4671393在中国儿童急性淋巴细胞白血病中的保护作用
Francisco Javier Borrayo-LóPez,Bertha Ibarra-Cortés,FranciscoJavier Perea-Díaz et al.
Francisco Javier Borrayo-LóPez et al.
In acute lymphoblastic leukaemia (ALL), elevated foetal haemoglobin (HbF) levels have been associated with the prognosis of patients. Genetic variants in HbF regulatory genes: BAF chromatin remodelling complex subunit (BCL11A), HBS1L-MYB tr...
Genetic characterization and linkage analysis of spotted leaf 6,liguleless and lax panicle traits in mutant rice [0.03%]
水稻斑叶6号、无叶舌和松散花序等突变体的遗传分析及基因定位研究
Mohammad Nurul Matin,Kyung Eun Lee,Sang Gu Kang
Mohammad Nurul Matin
Phenotypic mutants are valuable resources for elucidating the function of genes responsible for their expression. This study examined mutant rice strains expressing three traits: spotted leaf 6 (spl6), lax panicle (lax), and liguleless (lg)...
Oliver Mayo,Vidyanand Nanjundiah
Oliver Mayo
A recent report by G. Clark points to a sustained persistence of social status in England that extends vertically across several generations and horizontally across many levels of kinship. We seek to put his findings in historical perspecti...
Genetic analysis of a child with severe intellectual disability caused by a novel variant in the FERM domain of the FRMPD4 protein [0.03%]
遗传分析一种由蛋白质FRMPD4的FERM域新型变异引起的严重智力障碍患儿病例
Hua Pan,Feng Zhu,Kun Chen et al.
Hua Pan et al.
Intellectual developmental disorder, X-linked 104 (XLID104), caused by the FRMPD4 gene variant, is a rare X-linked genetic disease that primarily manifests as intellectual disability (ID) and language delay, and may be accompanied by behavi...
Case Reports
Journal of genetics. 2024:103:14. DOI: 2024
Multiple mutations in BADH2 gene reveal the novel fragrance allele in indica rice (Oryza sativa L.) [0.03%]
坏血病2基因多位点突变揭示了水稻中的新型香味等位基因
Sonali Chandanshive,Sarika Mathure,Altafhusain Nadaf
Sonali Chandanshive
The aroma in rice is the most appreciable quality trait, controlled by the loss of function of the betaine aldehyde dehydrogenase 2 (BADH2) gene. In the present study, indica rice cultivars (basmati, nonbasmati aromatic, and nonaromatic) we...